Actively Recruiting
CCSV - Post Market Clinical Follow-up Study
Led by Medical University of Vienna · Updated on 2025-02-20
98
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
Sponsors
M
Medical University of Vienna
Lead Sponsor
W
WEINMANN Emergency, Medical Technology GmbH & Co. KG
Collaborating Sponsor
AI-Summary
What this Trial Is About
The main goal of this observational study is the evaluation of Chest Compression Synchronized Ventilation (CCSV) regarding oxygenation in terms of PaO2 assessed by routine blood gas analysis, hemodynamic effects, 30-day outcome and safety in comparison to Intermittent Positive Pressure Ventilation (IPPV) as data in humans is sparse especially in direct comparison to other ventilation modes. Cardiac arrest patients in Vienna, Austria will be preclinically randomized (IPPV and CCSV) and ventilated accordingly during CPR. Differences in oxygenation, decarboxylation, systemic perfusion and cerebral oxygenation, the patient's 30-day outcome as well as ventilator-associated adverse events (e.g., pneumothorax) will be recorded and analyzed.
CONDITIONS
Official Title
CCSV - Post Market Clinical Follow-up Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cardiac arrest occurred outside of a hospital (OHCA)
- Correct placement of breathing tube confirmed by capnography
- Emergency ventilation treatment provided by Vienna Emergency Medical Services
- Use of MEDUMAT Standard device from Weinmann Emergency
- Mechanical ventilation performed according to specified indications
You will not qualify if you...
- Eligible for extracorporeal cardiopulmonary resuscitation (eCPR) as defined by Vienna Emergency Medical Service
- Recovery with sustained return of spontaneous circulation before or within first 3 minutes of mechanical ventilation
- Mechanical ventilation started before study inclusion during ongoing CPR
- Traumatic cardiac arrest
- Suspected or known pregnancy
- Clinically suspected tension or non-tension pneumothorax
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Medical University of Vienna
Vienna, Austria, Austria, 1090
Actively Recruiting
Research Team
S
Sebastian Schnaubelt, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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